Cell, colony-forming

DL-CFU Dendritic cell/Langerhans cell colony forming DLE Discoid lupus erythematosus DMARD Disease-modifying antirheumatic drug... 

Although exopolysaccharides do not normally have a structural role, they do form structures that can be detected by either light or electron microscopy. Exopolysaccharides may form part of a capsule closely attached to the microbial cell surface, or appear as loose slime secreted by the cell but not directly attached to it mucoid Exopolysaccharide producing cells usually form mucoid colonies on solid media and colonies liquid cultures of these cells may become very viscous. However, growth conditions can... 

All mature blood cells arise from primitive hematopoietic cells in the bone marrow, the pluripotent stem cells. Approximately 0.1% of the nucleated cells of the bone marrow are pluripotent stem cells and approximately 5% of these cells may be actively cycling at any one time. The stem cell pool maintains itself through a process of asymmetrical cell division when a stem cell divides, one daughter cell remains a stem cell and the other becomes a committed colony-forming cell (CFC). The proliferation and differentiation of CFCs are controlled by hematopoietic growth factors. The hematopoietic growth factors stimulate cell division, differentiation and maturation, and convert the dividing cells into a population of terminally differentiated functional cells. 

E.coli recA y.luxCDABE strain were grown for 16-18 hours at 37°C in LB-broth in the presence of 20 pg/ ml of ampicillin. Immediately before the experiment the culture was diluted 1 20 by fresh culture medium and incubated until early log-phase. The grown biomass was mixed with AR solutions in final concentrations of ICfs, ICH n ICfs M, with used for their dilution with distilled water (control) and incubated for 60 minutes. The luminescence intensity of UV-irradiated E.coli recA lux and intact specimens were registered by plate bioluminometer LM OIT (Immimotech, Czech Rep.) in a real time. The number of viable cells was determined from the colony-forming units (CFU) on a surface of a LB-agar after the subsequent incubation within 24 hours at 37 °C. A quantitative estimation of an induction of the SOS-system calculated on formula... 

Fig. 2.4 The budding pattern in haploid and diploid Saccharomyces cerevisiae. The original cell which formed a bud is the mother (M). The daughter cell (D) is shown remaining attached as might be the case in i colonies growing on the surface of agar.

Studies by Hudson et al, (2000) have demonstrated the presence of eight polyphenols in rice bran by using high-pressure liquid chromatography. They are protocatechuic acid, p-coumaric acid, ferulic acid, sinapic aci vanillic acid, caffeic acid, which is a methoxycirmamic acid derivative, and tricin. The effect of these polyphenols on cell viability and on the colony-forming ability of human-derived MDA MB 468 and HBL 100 breast cells, colon-derived SW 480 and human colonic epithelial cells was assessed. These authors concluded that rice bran polyphenols have putative cancer chemopreventive properties. 

BCF Basophil chemotactic factor B-CFC Basophil colony-forming cell BCG Bacillus Calmette-Guerin BCNU l,3-bis(2-chloroethyl)-l-nitrosourea bFGF Basic fibroblast growth fiictor Bg Birbeck granules BHR Bronchial hyperresponsiveness BHT Butylated hydroxyroluene b.i.d. Bis in die (twice a day)... 

A number of biochemical markers not associated with the cell envelope allow the specific detection of individual microorganisms in environmental samples. These include secondary alcohols. For example, Mycobacterium xenopi can be detected through the hydrolysis of wax ester mycolates, which liberates 2-docosanol, a characteristic and dominant secondary alcohol, which can be detected at low levels by GC-MS. This biomarker was found to be very useful for the rapid detection of M. xenopi in drinking water (159,160). Results from the GC-MS detection of 2-docosanol were obtained within 2 days compared to the 12 weeks required for culturable detection of M. xenopi. The detection limit for this type of approach was found to be 10 colony-forming units (CFU) ml" drinking water. 

Erythropoiesis is a process that starts with a pluripotent stem cell in the bone marrow that eventually differentiates into an erythroid colony-forming unit (CFU-E)4 (Fig. 63-1). The development of these cells depends on stimulation from the appropriate growth factors, primarily erythropoietin. Other cytokines involved include granulocyte-monocyte colony-stimulating factor (GM-CSF) and interleukin 3 (IL-3). Eventually, the CFU-Es differentiate into reticulocytes and cross from the bone marrow into the peripheral blood. Finally, these reticulocytes mature into erythrocytes after 1 to 2 days in the bloodstream. Throughout this process, the cells gradually accumulate more hemoglobin and lose their nuclei.4... 

Moore MA, Metcalf D. Ontogeny of the haemopoietic system yolk sac origin of in vivo and in vitro colony forming cells in the developing mouse embryo. Br J Haematol 1970 18(3) 279-296. 

The most common criticism of whole-cell MALDI is that the method requires a relatively large number of cells, usually obtained directly from culture media. In principle, an analysis of even a few unknown bacteria (a colony-forming unit) is possible after a culture step. More important is the number of bacteria needed in a sample or on the sample probe for successful analysis. Detection of a very small number of bacteria could eliminate the need for a preliminary culture step. This would be a considerable asset for environmental analysis (unless to many bacteria were detected) and for the detection of a bioterrorism-related release of bacteria. 

Faeces from colonised cows may contain from 102 to 107 colony-forming units (CFU) of Salmonella cells per gram of faeces. Particularly calves and heifers colonised with E. coli 0157 H7 may shed the bacteria at levels ranging from 102 to 105 CFU g 1 (Himathongham el al., 1999). Furthermore, calves younger than four months are the main domestic animals that excrete pathogenic protozoa like Giardia and Cryptosporidia. 

ES cell colony which was formed after ES cell colony and derived recovering from the PMBV/PVA hydrogel, (differentiated) cells which... 

The sensitivity obtained with ATP BL is around 1000-10,000 colony-forming units (CFU) per milliliter. Better detection was obtained by determining adenylate kinase instead of ATP 10-1000 cells/100 iL [71]. 

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